Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_provenance.
- NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_assertion description "[Inactivating HRPT2 mutations are common in HPT- JT and parathyroid carcinomas, and have been described in a few cases of parathyroid adenomas with cystic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_provenance.
- NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_assertion evidence source_evidence_literature NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_provenance.
- NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_assertion SIO_000772 16728578 NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_provenance.
- NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_assertion wasDerivedFrom befree-20140225 NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_provenance.
- NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_assertion wasGeneratedBy ECO_0000203 NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP208338.RA8Xe3wHz4Jdh8t9ZRZ-frzRWIDXWEUcwB9zTcJjOLZNs130_provenance.